Thong Melissa S Y, Wolschon Eva-Maria, Koch-Gallenkamp Lena, Waldmann Annika, Waldeyer-Sauerland Mechthild, Pritzkuleit Ron, Bertram Heike, Kajüter Hiltraud, Eberle Andrea, Holleczek Bernd, Zeissig Sylke R, Brenner Hermann, Arndt Volker
Unit of Cancer Survivorship, Division of Clinical Epidemiology and Aging Research, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Institute for Social Medicine and Epidemiology, University of Lübeck, Lübeck, Germany.
JNCI Cancer Spectr. 2018 Jul 5;2(2):pky031. doi: 10.1093/jncics/pky031. eCollection 2018 Apr.
The concept of cancer identity is gaining attention as more individuals are living with cancer as a chronic illness. Research is limited, and results suggest that a self-identity as "cancer patient" rather than a "cancer survivor" is associated with depression and lower health-related quality of life (HRQL). We aimed to identify factors associated with patient identity and investigate the associations between patient identity and treatment, health care use, psychosocial distress, and HRQL.
We used data from the population-based CAncEr Survivorship: A multi-Regional (CAESAR) study. Breast, colorectal, and prostate cancer survivors diagnosed during 1994-2004 completed a postal survey on patient identity, HRQL, psychological distress, and health care use in 2009-2011. We calculated odds ratios and the 95% confidence interval of having a patient identity. Analyses were adjusted for age, sex, education, and cancer stage, where appropriate.
Of the 6057 respondents, colorectal cancer survivors (25%) were least likely to consider themselves patients, and prostate cancer survivors (36%) the most likely. Being male, younger age, comorbidity, higher cancer stage, and disease recurrence were associated with patient identity. Treatment was associated with patient identity, except among female colorectal cancer survivors. Having a patient identity was associated with higher health care use within the past 12 months. Survivors who still consider themselves patients were more likely to be depressed and reported significantly lower HRQL.
A significant proportion of cancer survivors still consider themselves patients five to 15 years postdiagnosis. Sensitivity to individuals' self-identity should be considered when exploring their cancer experience.
随着越来越多的人以慢性病的形式与癌症共存,癌症身份的概念受到了更多关注。相关研究有限,结果表明,将自己视为“癌症患者”而非“癌症幸存者”与抑郁及较低的健康相关生活质量(HRQL)有关。我们旨在确定与患者身份相关的因素,并调查患者身份与治疗、医疗保健使用、心理社会困扰及HRQL之间的关联。
我们使用了基于人群的癌症幸存者:多地区(CAESAR)研究的数据。1994年至2004年期间被诊断出患有乳腺癌、结直肠癌和前列腺癌的幸存者在2009年至2011年完成了一项关于患者身份、HRQL、心理困扰和医疗保健使用的邮寄调查。我们计算了具有患者身份的比值比和95%置信区间。在适当情况下,分析对年龄、性别、教育程度和癌症分期进行了调整。
在6057名受访者中,结直肠癌幸存者(25%)最不可能将自己视为患者,而前列腺癌幸存者(36%)最有可能。男性、年轻、合并症、癌症分期较高和疾病复发与患者身份有关。治疗与患者身份有关,但女性结直肠癌幸存者除外。在过去12个月内,具有患者身份与更高的医疗保健使用有关。仍将自己视为患者的幸存者更有可能抑郁,且报告的HRQL显著更低。
相当一部分癌症幸存者在确诊后5至